614 results on '"Vorgerd M"'
Search Results
52. Integration proteomischer und genetischer Daten zur Pathogeneseforschung bei der sporadischen Einschlusskörpermyositis (sIBM)
53. Reduced intracortical facilitation in patients with cerebellar degeneration
54. Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease)
55. Mitochondrial impairment of human muscle in Friedreich ataxia in vivo
56. Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease)
57. Reliability of DTI-based muscle-volumetry as compared to conventional T1-based manual segmentation
58. VALUE OF SMALL FIBER NEUROPATHY IN FIBROMYALGIA PATIENTS IN A RHEUMATOLOGICAL SETTING.
59. Differential roles of hypoxia and innate immune mechanisms in juvenile and adult dermatomyositis
60. Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P
61. P.120EUROMAC: A European registry for patients with McArdle disease and other very rare muscle glycogenoses
62. Hereditary rippling muscle disease is caused by caveolin-3 mutations
63. Therapie der Muskeldystrophien/das Deutsche Muskeldystrophie- Netzwerk (MD-NET)
64. Autoimmune rippling muscle disease: IgG antibodies bind to human muscle fibers
65. FV 9. Diffusion Tensor Imaging in Neuromuscular diseases - A novel method for quantification of muscle degeneration in myopathy patients
66. Differential analysis of protein aggregates in myofibrillar myopathies – a proteomic approach
67. LMD-assisted Comparison of Muscle Proteome in Patients with Filaminopathy and matched Controls
68. Autoimmune Rippling Muscle Disease – Histologische Auffälligkeiten und Bindungsstudien
69. Muskelschmerzen bei der Mc Ardle-Erkrankung (Glykogenose TypV)
70. Mitochondrial impairment in patients and asymptomatic gene carriers of Huntington's disease
71. Molekulare Pathomechanismen der Filaminopathie: funktionelle Charakterisierung der p.W2710X Mutation
72. Muskuläre Ermüdung und kortikale Exzitabilitätsveränderungen bei Patienten mit Muskeldystrophie und Fibromyalgie-Syndrom: Eine Studie mit transkranieller Magnetstimulation
73. Symptomatische Konduktorinnen einer Adrenoleukodystrophie/Adrenomyeloneuropathie: Eine ungewöhnliche Konstellation in einer deutschen ALD/AMN- Familie
74. Charakterisierung des klinischen und morphologischen Phänotyps der Filaminopathie
75. Therapie der autoimmunen Myasthenia gravis mit Rituximab: eine offene Beobachtungsstudie
76. New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses
77. Roles of hypoxia and innate immune mechanisms in juvenile and adult dermatomyositis
78. P.99 - Reliability of DTI-based muscle-volumetry as compared to conventional T1-based manual segmentation
79. Phenylketonuria: distribution of DNA diagnostic patterns in German families
80. Magnetresonanzspektroskopie der Skelettmuskulatur
81. Long survival in leigh syndrome: new cases and review of literature
82. G.P.69
83. G.P.256
84. G.P.64
85. G.P.245
86. A.P.2
87. A.P.3
88. P70 EUROMAC: Disease registry for McArdle disease and other pure muscle glycogenolytic disorders presenting with exercise intolerance
89. Effect of high-dose creatine therapy on symptoms of exercise intolerance in McArdle disease
90. Muskelglykogenosen, Klinik, Diagnostik und Therapie
91. Near infrared spectroscopy applied to meatbolic myopathies: a combined MRS and NIRS approach
92. Near infrared spectroscopy applied to metabolic myopathies: a combined MRS and NIRS approach
93. Creatine supplementation results in elevated PCr/ATP ratios in the calf muscle of athletes but not in patients with myopathies
94. Glycogen breakdown during isometric contraction in perfused and ischaemic PFK-deficient human leg muscle
95. The impaired oxidative energy metabolism in the calf muscle of immobilised healthy subjects and patients with Friedreich's ataxia and Huntington's disease
96. Creatine Therapy in Myophosphorylase Deficiency (McArdle Disease)
97. Metabolic and electrophysiologic phenotype in myophosphorylase deficiency (Glycogenosis Type V, McArdle's disease)
98. Mitochondrial impairment of human muscle in Friedreich's ataxia in vivo
99. P.396 - Autoimmune rippling muscle disease: IgG antibodies bind to human muscle fibers
100. A placebo-controlled crossover trial of creatine therapy in myophosphorylase deficiency (McArdle's disease)
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